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rs397514497

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514497(G;T)
Make rs397514497(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position202514941
GeneBMPR2
is asnp
is mentioned by
dbSNPrs397514497
ebirs397514497
HLIrs397514497
Exacrs397514497
Varsomers397514497
Maprs397514497
PheGenIrs397514497
hapmaprs397514497
1000 genomesrs397514497
hgdprs397514497
ensemblrs397514497
gopubmedrs397514497
geneviewrs397514497
scholarrs397514497
googlers397514497
pharmgkbrs397514497
gwascentralrs397514497
openSNPrs397514497
23andMers397514497
23andMe allrs397514497
SNP Nexus

SNPshotrs397514497
SNPdbers397514497
MSV3drs397514497
GWAS Ctlgrs397514497
Max Magnitude0
ClinVar
Risk rs397514497(A,T;A,T)
Alt rs397514497(A,T;A,T)
Reference rs397514497(G;G)
Significance Pathogenic
Disease Pulmonary venoocclusive disease 1
Variation info
Gene BMPR2
CLNDBN Pulmonary venoocclusive disease 1
Reversed 0
HGVS NC_000002.11:g.203379664G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032618.3,